esv3641803

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:72
Validation:Not tested
Clinical Assertions: No
Region Size:31,610

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 443 SVs from 56 studies. See in: genome view

Remapped(Score: Perfect):11,613,646-11,645,255

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3641803	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
esv3641803	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	11,613,645	11,645,254

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv15807257	copy number loss	SAMN00004648	Sequencing	Read depth and paired-end mapping	Heterozygous	2,529
essv15807258	copy number loss	SAMN00006520	Sequencing	Read depth and paired-end mapping	Heterozygous	2,560
essv15807259	copy number loss	SAMN01036851	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv15807260	copy number loss	SAMN00006574	Sequencing	Read depth and paired-end mapping	Heterozygous	2,657
essv15807261	copy number loss	SAMN00006582	Sequencing	Read depth and paired-end mapping	Heterozygous	2,646
essv15807262	copy number loss	SAMN00006585	Sequencing	Read depth and paired-end mapping	Heterozygous	2,864
essv15807263	copy number loss	SAMN00249889	Sequencing	Read depth and paired-end mapping	Heterozygous	2,824
essv15807264	copy number loss	SAMN00009122	Sequencing	Read depth and paired-end mapping	Heterozygous	2,787
essv15807265	copy number loss	SAMN01091085	Sequencing	Read depth and paired-end mapping	Heterozygous	2,184
essv15807266	copy number loss	SAMN00009142	Sequencing	Read depth and paired-end mapping	Heterozygous	2,904
essv15807267	copy number loss	SAMN00009189	Sequencing	Read depth and paired-end mapping	Heterozygous	2,550
essv15807268	copy number loss	SAMN00009190	Sequencing	Read depth and paired-end mapping	Heterozygous	2,590
essv15807269	copy number loss	SAMN01091069	Sequencing	Read depth and paired-end mapping	Heterozygous	2,643
essv15807270	copy number loss	SAMN01091125	Sequencing	Read depth and paired-end mapping	Heterozygous	2,183
essv15807271	copy number loss	SAMN01761633	Sequencing	Read depth and paired-end mapping	Heterozygous	2,248
essv15807272	copy number loss	SAMN00249775	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv15807273	copy number loss	SAMN00255150	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv15807274	copy number loss	SAMN00249856	Sequencing	Read depth and paired-end mapping	Heterozygous	2,571
essv15807275	copy number loss	SAMN01761398	Sequencing	Read depth and paired-end mapping	Heterozygous	2,294
essv15807276	copy number loss	SAMN01096674	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv15807277	copy number loss	SAMN01096757	Sequencing	Read depth and paired-end mapping	Heterozygous	2,635
essv15807278	copy number loss	SAMN01096765	Sequencing	Read depth and paired-end mapping	Heterozygous	2,584
essv15807279	copy number loss	SAMN00800947	Sequencing	Read depth and paired-end mapping	Heterozygous	2,732
essv15807280	copy number loss	SAMN00801049	Sequencing	Read depth and paired-end mapping	Heterozygous	2,553
essv15807281	copy number loss	SAMN00000436	Sequencing	Read depth and paired-end mapping	Heterozygous	2,689
essv15807282	copy number loss	SAMN00000458	Sequencing	Read depth and paired-end mapping	Heterozygous	2,797
essv15807283	copy number loss	SAMN00001064	Sequencing	Read depth and paired-end mapping	Heterozygous	2,799
essv15807284	copy number loss	SAMN00001163	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv15807285	copy number loss	SAMN00007777	Sequencing	Read depth and paired-end mapping	Heterozygous	2,181
essv15807286	copy number loss	SAMN00001240	Sequencing	Read depth and paired-end mapping	Heterozygous	2,871
essv15807287	copy number loss	SAMN00001288	Sequencing	Read depth and paired-end mapping	Heterozygous	2,516
essv15807288	copy number loss	SAMN00001309	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv15807289	copy number loss	SAMN00001324	Sequencing	Read depth and paired-end mapping	Heterozygous	2,810
essv15807290	copy number gain	SAMN00004647	Sequencing	Read depth and paired-end mapping	Homozygous	2,660
essv15807291	copy number gain	SAMN00014422	Sequencing	Read depth and paired-end mapping	Heterozygous	2,642
essv15807292	copy number gain	SAMN00249824	Sequencing	Read depth and paired-end mapping	Heterozygous	2,701
essv15807293	copy number gain	SAMN00249741	Sequencing	Read depth and paired-end mapping	Heterozygous	2,483
essv15807294	copy number gain	SAMN00249738	Sequencing	Read depth and paired-end mapping	Heterozygous	2,682
essv15807295	copy number gain	SAMN01036773	Sequencing	Read depth and paired-end mapping	Heterozygous	2,954
essv15807296	copy number gain	SAMN01096723	Sequencing	Read depth and paired-end mapping	Heterozygous	2,577
essv15807297	copy number gain	SAMN01090981	Sequencing	Read depth and paired-end mapping	Heterozygous	2,866
essv15807298	copy number gain	SAMN01090982	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv15807299	copy number gain	SAMN01090985	Sequencing	Read depth and paired-end mapping	Heterozygous	2,681
essv15807300	copy number gain	SAMN01090986	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv15807301	copy number gain	SAMN01091018	Sequencing	Read depth and paired-end mapping	Heterozygous	2,713
essv15807302	copy number gain	SAMN01761581	Sequencing	Read depth and paired-end mapping	Heterozygous	2,794
essv15807303	copy number gain	SAMN01096783	Sequencing	Read depth and paired-end mapping	Heterozygous	2,691
essv15807304	copy number gain	SAMN01096686	Sequencing	Read depth and paired-end mapping	Heterozygous	2,657
essv15807305	copy number gain	SAMN01761508	Sequencing	Read depth and paired-end mapping	Heterozygous	2,844
essv15807306	copy number gain	SAMN01096791	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv15807307	copy number gain	SAMN01096787	Sequencing	Read depth and paired-end mapping	Homozygous	2,756
essv15807308	copy number gain	SAMN01091019	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv15807309	copy number gain	SAMN01090984	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv15807310	copy number gain	SAMN01090998	Sequencing	Read depth and paired-end mapping	Heterozygous	2,627
essv15807311	copy number gain	SAMN01090988	Sequencing	Read depth and paired-end mapping	Heterozygous	2,742
essv15807312	copy number gain	SAMN01096719	Sequencing	Read depth and paired-end mapping	Heterozygous	2,696
essv15807313	copy number gain	SAMN01091003	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv15807314	copy number gain	SAMN01096720	Sequencing	Read depth and paired-end mapping	Heterozygous	2,511
essv15807315	copy number gain	SAMN01091035	Sequencing	Read depth and paired-end mapping	Heterozygous	2,577
essv15807316	copy number gain	SAMN01096777	Sequencing	Read depth and paired-end mapping	Heterozygous	2,589
essv15807317	copy number gain	SAMN01761573	Sequencing	Read depth and paired-end mapping	Heterozygous	2,198
essv15807318	copy number gain	SAMN01761566	Sequencing	Read depth and paired-end mapping	Homozygous	2,183
essv15807319	copy number gain	SAMN01761493	Sequencing	Read depth and paired-end mapping	Heterozygous	2,931
essv15807320	copy number gain	SAMN01761583	Sequencing	Read depth and paired-end mapping	Heterozygous	2,864
essv15807321	copy number gain	SAMN00801055	Sequencing	Read depth and paired-end mapping	Heterozygous	2,803
essv15807322	copy number gain	SAMN00001654	Sequencing	Read depth and paired-end mapping	Heterozygous	2,454
essv15807323	copy number gain	SAMN00001662	Sequencing	Read depth and paired-end mapping	Heterozygous	2,113
essv15807324	copy number gain	SAMN00000517	Sequencing	Read depth and paired-end mapping	Heterozygous	2,733
essv15807325	copy number gain	SAMN00007716	Sequencing	Read depth and paired-end mapping	Heterozygous	2,449
essv15807326	copy number gain	SAMN00001224	Sequencing	Read depth and paired-end mapping	Heterozygous	2,786
essv15807327	copy number gain	SAMN00004495	Sequencing	Read depth and paired-end mapping	Heterozygous	2,687
essv15807328	copy number gain	SAMN00004498	Sequencing	Read depth and paired-end mapping	Heterozygous	2,749

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv15807257	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807258	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807259	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807260	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807261	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807262	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807263	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807264	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807265	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807266	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807267	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807268	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807269	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807270	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807271	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807272	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807273	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807274	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807275	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807276	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807277	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807278	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807279	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807280	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807281	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807282	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807283	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807284	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807285	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807286	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807287	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807288	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807289	Remapped	Perfect	NC_000018.10:g.116 13646_11645255del	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807290	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807291	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807292	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807293	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807294	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807295	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807296	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807297	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807298	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807299	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807300	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807301	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807302	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807303	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807304	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807305	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807306	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807307	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807308	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807309	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807310	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807311	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807312	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807313	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807314	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807315	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807316	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807317	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807318	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807319	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807320	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807321	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807322	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807323	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807324	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807325	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807326	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807327	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807328	Remapped	Perfect	NC_000018.10:g.116 13646_11645255dup	GRCh38.p12	First Pass	NC_000018.10	Chr18	11,613,646	11,645,255
essv15807257	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807258	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807259	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807260	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807261	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807262	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807263	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807264	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807265	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807266	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807267	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807268	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807269	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807270	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807271	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807272	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807273	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807274	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807275	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807276	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807277	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807278	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807279	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807280	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807281	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807282	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807283	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254
essv15807284	Submitted genomic		NC_000018.9:g.1161 3645_11645254del	GRCh37 (hg19)		NC_000018.9	Chr18	11,613,645	11,645,254

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dbVar

Database of genomic structural variation

esv3641803

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.